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A reexamination of unsaturated carboxylate dianion reactions. Evidence for α- and γ- substitutions in alkenoic acids

✍ Scribed by Philip E. Pfeffer; Leonard S. Silbert; Edward Kinsel


Book ID
104246747
Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
245 KB
Volume
14
Category
Article
ISSN
0040-4039

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✦ Synopsis


In our previous studiesL on the preparation and reactions of dianions (Equation l), we reported the quantitative conversion of cr, B-unsaturated carboxylic acids (I) to their S, Y-isomers (III) through formation of the stable intermediate dianion (II). The dianions were prepared by reaction of the appropriate carboxylic acid with lithium diisopropylamide (butyl lithium-diisopropylamine) in


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